Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7022547 | 7613044 | I | 7022547-4 | 20100101 | 20100928 | 20100930 | EXP | CN-PFIZER INC-2010122638 | PFIZERINC | 58 | YR | F | Y | 20100929 | LW | CHINA |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7022547 | 1014810094 | PS | MEDROL | 1 | ORAL | 12 TABLETS DAILY | 011153 | ||||
| 7022547 | 1014810095 | SS | MEDROL | 1 | ORAL | 5 TABLETS DAILY | 011153 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7022547 | 1014810094 | NEPHROTIC SYNDROME |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7022547 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 7022547 | GENERALISED OEDEMA |
| 7022547 | MEDICATION ERROR |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7022547 | 1014810094 | 20100101 | |||
| 7022547 | 1014810095 | 20100101 |